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Bidisha Saha

Showing results (21-30 of 25) with videos related to

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Journal of the American Society of Nephrology : JASN|March 9, 2023
Potassium Activates mTORC2-dependent SGK1 Phosphorylation to Stimulate Epithelial Sodium Channel: Role in Rapid Renal Responses to Dietary PotassiumBidisha Saha, Waheed Shabbir, Enzo Takagi, et al.
Kidney International|April 25, 2026
Roles of WNK1 and mTORC2 in aldosterone-independent regulation of potassium secretion in the distal nephronBidisha Saha, Enzo Takagi, Cheng-Biao Zhang, et al.
Human Mutation|July 15, 2015
POLD1 Germline Mutations in Patients Initially Diagnosed with Werner SyndromeDavor Lessel, Fuki M Hisama, Katalin Szakszon, et al.
The Journal of Clinical Investigation|August 29, 2017
Dysfunction of the MDM2/p53 axis is linked to premature agingDavor Lessel, Danyi Wu, Carlos Trujillo, et al.
Human Genetics|May 6, 2010
WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterationsKatrin Friedrich, Lin Lee, Dru F Leistritz, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Journal of the American Society of Nephrology : JASN|March 9, 2023
Potassium Activates mTORC2-dependent SGK1 Phosphorylation to Stimulate Epithelial Sodium Channel: Role in Rapid Renal Responses to Dietary PotassiumBidisha Saha, Waheed Shabbir, Enzo Takagi, et al.
Kidney International|April 25, 2026
Roles of WNK1 and mTORC2 in aldosterone-independent regulation of potassium secretion in the distal nephronBidisha Saha, Enzo Takagi, Cheng-Biao Zhang, et al.
Human Mutation|July 15, 2015
POLD1 Germline Mutations in Patients Initially Diagnosed with Werner SyndromeDavor Lessel, Fuki M Hisama, Katalin Szakszon, et al.
The Journal of Clinical Investigation|August 29, 2017
Dysfunction of the MDM2/p53 axis is linked to premature agingDavor Lessel, Danyi Wu, Carlos Trujillo, et al.
Human Genetics|May 6, 2010
WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterationsKatrin Friedrich, Lin Lee, Dru F Leistritz, et al.
Pageof 3